"Labcorp Genetics (formerly Invitae), Labcorp"[submitter] AND "AMOT"[g - ClinVar - NCBI

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Items: 11

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 781558	NM_001113490.2(AMOT):c.3095C>T (p.Ala1032Val)	AMOT (A1032V +1 more)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 789145	NM_001113490.2(AMOT):c.2957C>T (p.Pro986Leu)	AMOT (P577L +1 more)	Single nucleotide variant (missense variant)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 734333	NM_001113490.2(AMOT):c.2946G>A (p.Pro982=)	AMOT	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 771229	NM_001113490.2(AMOT):c.2738_2764del (p.Val913_Pro921del)	AMOT	Deletion (inframe_deletion)	not provided	GBenign
Select item 715548	NM_001113490.2(AMOT):c.2683_2703del (p.Ala895_Ala901del)	AMOT	Deletion (inframe_deletion)	not provided	GLikely benign
Select item 725821	NM_001113490.2(AMOT):c.2695A>G (p.Thr899Ala)	AMOT (T899A +1 more)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 715211	NM_001113490.2(AMOT):c.2501C>A (p.Ala834Asp)	AMOT (A425D +1 more)	Single nucleotide variant (missense variant)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 777823	NM_001113490.2(AMOT):c.2340G>A (p.Ser780=)	AMOT	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 782827	NM_001113490.2(AMOT):c.1614G>A (p.Ser538=)	AMOT	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 723017	NM_001113490.2(AMOT):c.1401A>G (p.Thr467=)	AMOT	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 720806	NM_001113490.2(AMOT):c.948T>C (p.Ser316=)	AMOT	Single nucleotide variant (synonymous variant +1 more)	not provided	GBenign